Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap5 |
T |
C |
12: 52,566,406 (GRCm39) |
F1126L |
probably benign |
Het |
Arhgef11 |
G |
T |
3: 87,643,203 (GRCm39) |
A1472S |
probably benign |
Het |
Armc9 |
G |
A |
1: 86,184,992 (GRCm39) |
R681K |
probably benign |
Het |
Atxn2 |
T |
A |
5: 121,885,484 (GRCm39) |
|
probably null |
Het |
B3gnt6 |
C |
A |
7: 97,843,950 (GRCm39) |
L3F |
probably benign |
Het |
Cand2 |
A |
G |
6: 115,769,352 (GRCm39) |
T721A |
probably damaging |
Het |
Cntn2 |
A |
T |
1: 132,450,124 (GRCm39) |
M590K |
probably benign |
Het |
Cntn4 |
A |
T |
6: 106,644,418 (GRCm39) |
D622V |
probably damaging |
Het |
Des |
T |
G |
1: 75,337,272 (GRCm39) |
S71A |
probably benign |
Het |
Dnah5 |
C |
A |
15: 28,263,745 (GRCm39) |
R827S |
probably damaging |
Het |
Dstn |
G |
A |
2: 143,780,455 (GRCm39) |
G52S |
probably benign |
Het |
Eln |
T |
A |
5: 134,736,835 (GRCm39) |
R704* |
probably null |
Het |
Fezf2 |
T |
A |
14: 12,342,607 (GRCm38) |
K419N |
probably damaging |
Het |
Grin3a |
G |
A |
4: 49,665,501 (GRCm39) |
R1045* |
probably null |
Het |
Herc2 |
T |
A |
7: 55,856,326 (GRCm39) |
H3921Q |
probably damaging |
Het |
Hs3st2 |
A |
G |
7: 121,100,255 (GRCm39) |
E367G |
possibly damaging |
Het |
Hydin |
G |
A |
8: 111,325,616 (GRCm39) |
R4675H |
probably damaging |
Het |
Inhca |
A |
C |
9: 103,140,256 (GRCm39) |
Y488D |
possibly damaging |
Het |
Irf2bp1 |
T |
C |
7: 18,738,659 (GRCm39) |
S100P |
possibly damaging |
Het |
Itga10 |
A |
G |
3: 96,559,846 (GRCm39) |
I500M |
possibly damaging |
Het |
Kcnt2 |
T |
C |
1: 140,435,500 (GRCm39) |
V496A |
probably damaging |
Het |
Mansc1 |
T |
C |
6: 134,587,670 (GRCm39) |
D169G |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,741,835 (GRCm39) |
S3869T |
probably damaging |
Het |
Mrgprb4 |
G |
A |
7: 47,848,868 (GRCm39) |
T20I |
probably benign |
Het |
Nek4 |
A |
G |
14: 30,679,253 (GRCm39) |
E198G |
probably damaging |
Het |
Or12e8 |
G |
T |
2: 87,188,609 (GRCm39) |
V274L |
probably benign |
Het |
Or2y10 |
G |
A |
11: 49,455,129 (GRCm39) |
C127Y |
probably damaging |
Het |
Or5w11 |
C |
A |
2: 87,459,626 (GRCm39) |
T273K |
possibly damaging |
Het |
Ppfia4 |
A |
T |
1: 134,247,110 (GRCm39) |
F537I |
probably benign |
Het |
Rarb |
A |
G |
14: 16,434,293 (GRCm38) |
V295A |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 28,740,104 (GRCm39) |
S3941P |
probably damaging |
Het |
Scnn1b |
A |
G |
7: 121,511,698 (GRCm39) |
N370S |
probably damaging |
Het |
Stard9 |
C |
A |
2: 120,504,117 (GRCm39) |
S221R |
probably damaging |
Het |
Sv2c |
C |
T |
13: 96,126,319 (GRCm39) |
G311D |
probably damaging |
Het |
Tas2r109 |
T |
C |
6: 132,957,856 (GRCm39) |
I25V |
probably benign |
Het |
Tbcel |
A |
C |
9: 42,348,453 (GRCm39) |
I305S |
probably damaging |
Het |
Tmem35b |
A |
G |
4: 127,019,990 (GRCm39) |
|
probably null |
Het |
Tmem38b |
T |
C |
4: 53,840,765 (GRCm39) |
L60S |
probably damaging |
Het |
Tmtc4 |
A |
G |
14: 123,182,966 (GRCm39) |
I244T |
possibly damaging |
Het |
Usp9y |
C |
A |
Y: 1,394,002 (GRCm39) |
C576F |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,853,072 (GRCm39) |
N629K |
possibly damaging |
Het |
Vmn2r22 |
T |
C |
6: 123,614,363 (GRCm39) |
Y409C |
probably damaging |
Het |
Vmn2r-ps158 |
A |
G |
7: 42,674,142 (GRCm39) |
Y400C |
probably damaging |
Het |
|
Other mutations in Gm2381 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02309:Gm2381
|
APN |
7 |
42,472,033 (GRCm39) |
splice site |
probably benign |
|
R0266:Gm2381
|
UTSW |
7 |
42,469,372 (GRCm39) |
nonsense |
probably null |
|
R0617:Gm2381
|
UTSW |
7 |
42,469,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Gm2381
|
UTSW |
7 |
42,469,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R1340:Gm2381
|
UTSW |
7 |
42,469,828 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1549:Gm2381
|
UTSW |
7 |
42,471,825 (GRCm39) |
missense |
probably benign |
0.09 |
R1702:Gm2381
|
UTSW |
7 |
42,469,655 (GRCm39) |
missense |
probably benign |
0.08 |
R1708:Gm2381
|
UTSW |
7 |
42,469,649 (GRCm39) |
missense |
probably benign |
0.05 |
R1909:Gm2381
|
UTSW |
7 |
42,469,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R2848:Gm2381
|
UTSW |
7 |
42,469,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R2849:Gm2381
|
UTSW |
7 |
42,469,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R4437:Gm2381
|
UTSW |
7 |
42,469,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R5445:Gm2381
|
UTSW |
7 |
42,469,425 (GRCm39) |
missense |
probably damaging |
0.96 |
R5702:Gm2381
|
UTSW |
7 |
42,471,820 (GRCm39) |
missense |
probably benign |
0.12 |
R6370:Gm2381
|
UTSW |
7 |
42,470,010 (GRCm39) |
missense |
probably benign |
0.00 |
R6371:Gm2381
|
UTSW |
7 |
42,470,010 (GRCm39) |
missense |
probably benign |
0.00 |
R6372:Gm2381
|
UTSW |
7 |
42,470,010 (GRCm39) |
missense |
probably benign |
0.00 |
R6688:Gm2381
|
UTSW |
7 |
42,470,010 (GRCm39) |
missense |
probably benign |
0.00 |
R7150:Gm2381
|
UTSW |
7 |
42,469,888 (GRCm39) |
missense |
probably benign |
0.04 |
R7336:Gm2381
|
UTSW |
7 |
42,471,804 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8692:Gm2381
|
UTSW |
7 |
42,472,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R9658:Gm2381
|
UTSW |
7 |
42,469,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|